Department Summary
The intern will be a member of the GxP Supplier Management Chapter at Roche/Genentech and work with internal stakeholders at multiple Roche/Genentech sites, including Basel, Penzberg, Mannheim, South San Francisco, Vacaville, Singapore, Hillsboro and Oceanside. Overall, the intern will gain in-depth knowledge of the Roche/Genentech Quality requirements for externally sourced materials and products, GxP Supplier management processes, and GxP Supplier performance measurement tools. The intern will also support and develop processes and tools to enable PTQX teams to serve customers’ needs more effectively.
This internship position is located in South San Francisco.
Key Responsibilities
Support PTQX objectives and goals as well as PTQX processes
Improve material/product quality by working with GxP suppliers and PTQX teams-Initiate vendor changes in the Veeva system
Manage GxP supplier-related Quality issues
Provide support for GxP supplier business meetings
Intern will work with the Manager to refine deliverables and responsibilities based on intern’s capacity, interest level, and PTQX business needs
Program Highlights
Intensive 1 year, full-time (40 hours per week) paid internship.
Program start dates are in:
- Monday May 13, 2024
- Monday May 20, 2024
- Monday June 10, 2024
- Monday June 24, 2024
A stipend will be provided to help alleviate costs associated with the internship.
Ownership of challenging and impactful business-critical projects.
Work with some of the most talented people in the biotechnology industry.
Final presentations of project work to senior leaders.
Lead or participate in intern committees to design and coordinate program events and initiatives.
Professional & personal development curriculum throughout the program, including networking opportunities, workshops, and panel discussions.
Participate in volunteer projects, social events, and team-building activities.
Who You Are
Recent Bachelor’s graduates preferably in chemistry, biology, engineering, or business) with 0-2 years of experience in the pharmaceutical or biopharmaceutical industry, or an equivalent combination of education and experience
Preferably some knowledge of cGMP, GLP, or industry standards routinely used in the pharma industry (ISO, Federal Standards, etc.)
Preferably some knowledge of OE tools; e.g. statistical methods, FMEA, Six Sigma, Lean
Preferably some knowledge and/or experience in material sciences
Ability to interpret and follow Roche Quality standards
Ability to make sound decisions about scheduling, coordinating, and managing priorities
Strong interpersonal skills, which include a professional demeanor when interacting with personnel at all levels within Roche worldwide operations, suppliers, contract manufacturers, regulatory agency representatives, etc.
Flexibility in problem solving and work hours to meet business objectives
Requires excellent verbal and written communication skills, ability to influence others and work as part of a team
This position does not require domestic or international travel
Along with the submission of your CV, Please indicate your availability in your application.
The expected salary range for this position based on the primary location for this position of California is $33.00 – $45.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off benefits.
Relocation benefits are not available for this job posting.